Glucocorticoid-induced Tumor Necrosis Factor Receptor Is a p21 Transcriptional Target Conferring Resistance of Keratinocytes to UV Light-induced Apoptosis

Jian Wang, Vikram Devgan, Marcella Corrado, N S Prabhu, Wafik S. El‐Deiry, Carlo Riccardi, Pier Paolo Pandolfi, Caterina Missero, G. Paolo Dotto

Journal of Biological Chemistry · 2005 · 35 citations · 27 references

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Abstract

Glucocorticoid-induced tumor necrosis factor receptor (GITR) is a member of the tumor necrosis factor receptor superfamily, is expressed in T lymphocytes, and exerts an anti-apoptotic function in these cells. We reported that GITR is also highly expressed in the skin, specifically in keratinocytes, and that it is under negative transcriptional control of p21(Cip1/WAF1), independently from the cell cycle. Although GITR expression is higher in p21-deficient keratinocytes and skin, it is down-modulated with differentiation and in response to UVB. The combined analysis of keratinocytes with increased GITR expression versus normal keratinocytes and skin of mice with a disruption of the GITR gene indicates that this protein protects keratinocytes from UVB-induced apoptosis both in vitro and in vivo.

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